Application of OsRL7.1 protein to regulation and control of plant root development
A plant root and plant technology, applied in the fields of application, plant peptides, plant gene improvement, etc., can solve problems that affect the full utilization of cultivated land resources, difficult development of rice production, and impact on yield
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Embodiment 1
[0048] Example 1, the acquisition of rice OsRL7.1 and its sequence analysis
[0049] 1. Obtaining of rice OsRL7.1
[0050]Using 795 seedling-stage cultivated rice germplasms (including 506 indica and 289 japonica) as the association analysis population, the genotype and root length phenotype of the association analysis population were analyzed and identified. Specific steps are as follows:
[0051] 1. Phenotypic identification of the root length of the association analysis population by hydroponics
[0052] 1) First, after washing the seeds with sterile water, place them in a tissue culture room at 32°C for 64 hours to accelerate germination.
[0053] 2) For each variety, 5 seeds with normal germination and consistent growth potential were selected and transplanted to foam boards (30cm×42cm) with gauze as the bottom. Each foam board can plant 22 varieties (110 plants) and 20 rice plants as protection rows, and every two foam boards can be placed in the same blue plastic box...
Embodiment 2
[0060] Example 2, Obtaining of Rice OsRL7.1 Mutant and Functional Analysis of OsRL7.1
[0061] 1. Obtainment and identification of rice OsRL7.1 mutant
[0062] 1. Obtaining the rice OsRL7.1 mutant
[0063] Mutant Ti-OsRL7.1 was purchased from Korea Mutant Bank (URL: http: / / cbi.khu.ac.kr / RISD_DB.html), catalog number PFG_3A-03803.R. The OsRL7.1 mutant was identified by sequencing, and the T-DNA sequence was inserted into the promoter region of the OsRL7.1 gene.
[0064] 2. PCR identification of rice OsRL7.1 mutant
[0065] The primers were designed on the OsRL7.1 gene and T-DNA insert sequence to identify the rice OsRL7.1 mutant. The designed primers are shown in Table 1, wherein LP and RP are designed on the gene, and RB is designed at the RB (right border) end of the T-DNA insertion sequence.
[0066] Table 1. List of primers for identification of mutant systems
[0067] Primer
sequence
LP
5'GACGAGTCGAGACTGACACG
RP
5'CGCTAATAAGCCGTTATGG...
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